• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 < 
 1 
 2 
 3 
 4 
 
 
34 records meeting your search criteria returned- Product Code: KPN Product Problem: Inappropriate/Inadequate Shock/Stimulation Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
RODGER RODGER WIRELESS BEDWETTING ALARM 04/21/2017
MALEM MEDICAL MALEM BED WETTING ENURESIS ALARM FOR BOY 04/06/2017
MALEM MEDICAL LTD MALEM BED-WETTING ALARM 03/10/2017
MALEM MEDICAL MALEM ENURESIS ALARM 02/16/2016
-
-